HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Iodosuccinimide → 5-iodo-4-methyl-7H-pyrrolo[2,3-d]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 4-Methyl-7H-pyrrolo(2,3-d)pyrimidine | HCID 51341959 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-iodo-4-methyl-7H-pyrrolo[2,3-d]pyrimidine | HCID 58259299 | 76.2% |
Reaction Steps
To 4-methyl-7H-pyrrolo[2,3-d]pyrimidine (18, 0.634 g, 4.76 mmol) in 50 mL of dichloromethane, N-iodosuccinimide (1.3 g, 5.7 mmol) was added and the reaction stirred at room temperature for 45 minutes. The reaction was concentrated under vacuum, then ethyl acetate was added and washed with 1 N aqueous sodium thiosulfate. The organic layer was dried over sodium sulfate, filtered and the filtrate concentrated under vacuum. The resulting material was purified by silica gel column chromatography, eluting with 20-100% ethyl acetate in hexane. Appropriate fractions were combined and concentrated under vacuum to provide the desired compound (19, 0.94 g). MS (ESI) [M+H+]+=260.26.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09096593B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-96a101577cbc4cb9bc9cede27d7906fd |
| Source note | uspto-grants-2015_08 |